Canonical Allele Identifier: CA1728472100
Gene: LMTK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.98186844A= , CM000669.2:g.98186844A= GRCh38
NC_000007.13:g.97816156A= , CM000669.1:g.97816156A= GRCh37
NC_000007.12:g.97654092A= NCBI36
NG_013375.1:g.84960A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297293.6:c.877-33A= MANE Select ENSP00000297293.5:n.877-33A=
ENST00000297293.5:c.877-33A= ENSP00000297293.5:n.877-33A=
NM_014916.3:c.877-33A= NP_055731.2:n.877-33A=
XM_011515981.1:c.871-33A= XP_011514283.1:n.871-33A=
XM_011515981.3:c.871-33A= XP_011514283.1:n.871-33A=
NM_014916.4:c.877-33A= MANE Select NP_055731.2:n.877-33A=